Recurrent KIF2A mutations are responsible for classic lissencephaly

Cavallin, M.; Bijlsma, E.K.; Morjani, A. el; Moutton, S.; Peeters, E.A.J.; Maillard, C.; ... ; Bahi-Buisson, N. (2017)

Article / Letter to editor

• Lissencephaly
• Kinesin
• KIF2A

• All authors: Cavallin, M.; Bijlsma, E.K.; Morjani, A. el; Moutton, S.; Peeters, E.A.J.; Maillard, C.; Pedespan, J.M.; Guerrot, A.M.; Drouin-Garaud, V.; Coubes, C.; Genevieve, D.; Bole-Feysot, C.; Fourrage, C.; Steffann, J.; Bahi-Buisson, N.
• Date: 2017-04-30
• Journal: neurogenetics
• Volume: 18
• Issue: 2
• Pages: 73 - 79
• DOI: doi:10.1007/s10048-016-0499-8